Canonical Allele Identifier: CA430241915

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409127T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544400T>G , CM000664.2:g.178544400T>G	GRCh38
NC_000002.11:g.179409127T>G , CM000664.1:g.179409127T>G	GRCh37
NC_000002.10:g.179117373T>G	NCBI36
NG_011618.3:g.291403A>C , LRG_391:g.291403A>C
NG_051363.1:g.26574T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88125A>C (TTN)	ENSP00000343764.6:p.Gly29375=
ENST00000342175.11:c.69210A>C (TTN)	ENSP00000340554.6:p.Gly23070=
ENST00000359218.10:c.69009A>C (TTN)	ENSP00000352154.5:p.Gly23003=
ENST00000342175.10:c.69210A>C (TTN)	ENSP00000340554.6:p.Gly23070=
ENST00000342992.10:c.88125A>C (TTN)	ENSP00000343764.6:p.Gly29375=
ENST00000359218.9:c.69009A>C (TTN)	ENSP00000352154.5:p.Gly23003=
ENST00000460472.6:c.68634A>C (TTN)	ENSP00000434586.1:p.Gly22878=
ENST00000589042.5:c.95829A>C (TTN) MANE Select	ENSP00000467141.1:p.Gly31943=
ENST00000591111.5:c.90906A>C (TTN)	ENSP00000465570.1:p.Gly30302=
ENST00000615779.4:c.90906A>C (TTN)	ENSP00000483597.1:p.Gly30302=
NM_001256850.1:c.90906A>C (TTN)	NP_001243779.1:p.Gly30302=
NM_001267550.2:c.95829A>C (TTN) MANE Select	NP_001254479.2:p.Gly31943=
NM_003319.4:c.68634A>C (TTN)	NP_003310.4:p.Gly22878=
NM_133378.4:c.88125A>C (TTN)	NP_596869.4:p.Gly29375=
NM_133432.3:c.69009A>C (TTN)	NP_597676.3:p.Gly23003=
NM_133437.4:c.69210A>C (TTN)	NP_597681.4:p.Gly23070=
NR_038271.1:n.446+20764T>G (TTN-AS1)
NR_038272.1:n.2043+2039T>G (TTN-AS1)
XM_011511729.1:c.94926A>C (TTN)	XP_011510031.1:p.Gly31642=
XM_011511730.1:c.68820A>C (TTN)	XP_011510032.1:p.Gly22940=
XM_011511731.1:c.68679A>C (TTN)	XP_011510033.1:p.Gly22893=
XM_017004819.1:c.94722A>C (TTN)	XP_016860308.1:p.Gly31574=
XM_017004820.1:c.90120A>C (TTN)	XP_016860309.1:p.Gly30040=
XM_017004821.1:c.90117A>C (TTN)	XP_016860310.1:p.Gly30039=
XM_017004822.1:c.87159A>C (TTN)	XP_016860311.1:p.Gly29053=
XM_017004823.1:c.68775A>C (TTN)	XP_016860312.1:p.Gly22925=
XM_024453094.1:c.90270A>C (TTN)	XP_024308862.1:p.Gly30090=
XM_024453095.1:c.90267A>C (TTN)	XP_024308863.1:p.Gly30089=
XM_024453096.1:c.89700A>C (TTN)	XP_024308864.1:p.Gly29900=
XM_024453097.1:c.87042A>C (TTN)	XP_024308865.1:p.Gly29014=
XM_024453098.1:c.86961A>C (TTN)	XP_024308866.1:p.Gly28987=
XM_024453099.1:c.68724A>C (TTN)	XP_024308867.1:p.Gly22908=
XM_024453100.1:c.58578A>C (TTN)	XP_024308868.1:p.Gly19526=